Parkinsonian presentation in a child with Anti‐NMDAR Encephalitis.
- Published in:
- Movement Disorders Clinical Practice, 2025, v. 12, n. 5, p. 687, doi. 10.1002/mdc3.14336
- By:
- Publication type:
- Article
Works by Kumar, Ashna
Results: 18
1
2
Pulse methylprednisolone-induced sinus bradycardia: A rare but must know association.
- Published in:
- Indian Journal of Pharmacology, 2024, v. 56, n. 6, p. 440, doi. 10.4103/ijp.ijp_261_24
- By:
- Publication type:
- Article
3
Evaluation of Pediatric Leukodystrophies using Magnetic Resonance Imaging: A Prospective Study from North India.
- Published in:
- Medical Journal of Dr. D.Y. Patil Vidyapeeth, 2023, v. 16, n. 6, p. 962, doi. 10.4103/mjdrdypu.mjdrdypu_67_21
- By:
- Publication type:
- Article
4
Profile of Multisystem Inflammatory Syndrome in Children (MIS-C) in Infants in North India during the Second Wave of SARS-CoV-2 Pandemic.
- Published in:
- Indian Journal of Medical Specialities, 2024, v. 15, n. 3, p. 145, doi. 10.4103/injms.injms_196_23
- By:
- Publication type:
- Article
5
Neurodevelopmental Disorder with Spasticity, Hypomyelinating Leukodystrophy, and Brain Abnormalities (NEDSPLB) in an Indian Child.
- Published in:
- 2025
- By:
- Publication type:
- Letter
6
Acute Flaccid Paralysis due to Pyruvate Dehydrogenase E1-Alpha Deficiency.
- Published in:
- 2024
- By:
- Publication type:
- Letter
7
Skraban-Deardorff Syndrome in an Indian Child - A Very Rare Pathogenic Base Pair Deletion in WDR26 Gene.
- Published in:
- 2024
- By:
- Publication type:
- Letter
8
Knobloch Syndrome - Triad of Occipital Encephalocele, Retino-Choroidal Detachment and Epilepsy.
- Published in:
- 2024
- By:
- Publication type:
- Letter
9
Sedative for Sleep Electroencephalogram Records - A Debate of Ideal vs. Practical.
- Published in:
- 2023
- By:
- Publication type:
- Editorial
10
Childhood-Onset Neurodegeneration with Brain Atrophy in Association with c.628G>A in UBTF Gene.
- Published in:
- 2023
- By:
- Publication type:
- Letter
11
Developmental delay and assessment in an infant with PCWH syndrome: A case report.
- Published in:
- Annals of Movement Disorders, 2023, v. 6, n. 2, p. 96, doi. 10.4103/aomd.aomd_34_22
- By:
- Publication type:
- Article
12
Clinico-Etiologic Profile of Children and Adolescents with Drug-Resistant Epilepsy in a low-Resource Setting: 10 Years' Experience.
- Published in:
- Journal of Child Neurology, 2023, v. 38, n. 5, p. 315, doi. 10.1177/08830738231174493
- By:
- Publication type:
- Article
13
Spectrum of Movement Disorders Among Children With Subacute Sclerosing Panencephalitis: A Cross-Sectional Study.
- Published in:
- Journal of Child Neurology, 2022, v. 37, n. 6, p. 491, doi. 10.1177/08830738221085158
- By:
- Publication type:
- Article
14
Chromosome Xp22.3 deletion syndrome with X-linked ichthyosis, Kallmann syndrome, short stature, generalized epilepsy, hearing loss, attention deficit hyperactivity disorder, and intellectual disability - A rare report with review of literature.
- Published in:
- Journal of Neurosciences in Rural Practice, 2024, v. 15, n. 3, p. 425, doi. 10.25259/JNRP_467_2023
- By:
- Publication type:
- Article
15
Associated movement disorder as a clue for the diagnosis of paroxysmal kinesigenic dyskinesia in a child with focal epilepsy.
- Published in:
- Journal of Neurosciences in Rural Practice, 2023, v. 14, n. 3, p. 558, doi. 10.25259/JNRP_118_2023
- By:
- Publication type:
- Article
16
Familial hemiplegic migraine in Indian children—a tertiary center experience.
- Published in:
- Journal of Tropical Pediatrics, 2024, v. 70, n. 3, p. 1, doi. 10.1093/tropej/fmae008
- By:
- Publication type:
- Article
17
The Urokinase Plasminogen Activation System in Pancreatic Cancer: Prospective Diagnostic and Therapeutic Targets.
- Published in:
- Biomolecules (2218-273X), 2022, v. 12, n. 2, p. 152, doi. 10.3390/biom12020152
- By:
- Publication type:
- Article
18
MOGAD and Mortality: A Rarity.
- Published in:
- 2025
- By:
- Publication type:
- Letter to the Editor